rs2270744, MYH10

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35 0.010 1.000 1 2016 2016
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35 0.010 1.000 1 2016 2016
Retinoblastoma
CUI: C0035335
Disease: Retinoblastoma
193 1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35 0.010 1.000 1 2016 2016